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Investigation of modifier genes within copy number variations in Rett syndrome.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 5, p. 342, doi. 10.1038/jhg.2012.30
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- Publication type:
- Article
Investigation of modifier genes within copy number variations in Rett syndrome.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 7, p. 508, doi. 10.1038/jhg.2011.50
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- Publication type:
- Article
Analysis of the Phenotypes in the Rett Networked Database.
- Published in:
- International Journal of Genomics, 2019, p. 1, doi. 10.1155/2019/6956934
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- Publication type:
- Article
Combinatorial activation of the WNT‐dependent fibrogenic program by distinct complement subunits in dystrophic muscle.
- Published in:
- EMBO Molecular Medicine, 2023, v. 15, n. 12, p. 1, doi. 10.15252/emmm.202317405
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- Publication type:
- Article
Low‐level TP53 mutational load antecedes clonal expansion in chronic lymphocytic leukaemia.
- Published in:
- British Journal of Haematology, 2019, v. 184, n. 4, p. 657, doi. 10.1111/bjh.15147
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- Article